Author: Mentis, A.â€F. A.; Dardiotis, E.; Grigoriadis, N.; Petinaki, E.; Hadjigeorgiou, G. M.
Title: Viruses and endogenous retroviruses in multiple sclerosis: From correlation to causation Cord-id: svg3h2oi Document date: 2017_5_23
ID: svg3h2oi
Snippet: Multiple sclerosis is an immuneâ€mediated disease with an environmental component. According to a longâ€standing but unproven hypothesis dating to initial descriptions of multiple sclerosis (MS) at the end of the 19th century, viruses are either directly or indirectly implicated in MS pathogenesis. Whether viruses in MS are principally causal or simply contributory remains to be proven, but many viruses or viral elements—predominantly Epsteinâ€Barr virus, human endogenous retroviruses (HERV
Document: Multiple sclerosis is an immuneâ€mediated disease with an environmental component. According to a longâ€standing but unproven hypothesis dating to initial descriptions of multiple sclerosis (MS) at the end of the 19th century, viruses are either directly or indirectly implicated in MS pathogenesis. Whether viruses in MS are principally causal or simply contributory remains to be proven, but many viruses or viral elements—predominantly Epsteinâ€Barr virus, human endogenous retroviruses (HERVs) and human herpesvirus 6 (HHVâ€6) but also less common viruses such as Saffold and measles viruses—are associated with MS. Here, we present an upâ€toâ€date and comprehensive review of the main candidate viruses implicated in MS pathogenesis and summarize how these viruses might cause or lead to the hallmark demyelinating and inflammatory lesions of MS. We review data from epidemiological, animal and in vitro studies and in doing so offer a transdisciplinary approach to the topic. We argue that it is crucially important not to interpret “absence of evidence†as “evidence of absence†and that future studies need to focus on distinguishing correlative from causative associations. Progress in the MSâ€virus field is expected to arise from an increasing body of knowledge on the interplay between viruses and HERVs in MS. Such interactions suggest common HERVâ€mediated pathways downstream of viral infection that cause both neuroinflammation and neurodegeneration. We also comment on the limitations of existing studies and provide future research directions for the field.
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